Difference between revisions of "Part:BBa K2719000:Experience"

Revision as of 20:06, 17 October 2018

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Applications of BBa_K2719000

To confirm the presence of GST, it was cloned in pSB1C3 using EcoRI and PstI for the restriction and T4 ligase for the ligation. After that, it was transformed in Escherichia coli DH5a. (Figure 1)

Figure 1. Transformed GST Colonies

To prove the presence of the plasmid inside the colonies, two agarose gels were elaborated, one for watch the entire plasmid and the second one for the plasmid with a previously restriction process using NotI, so the last one could confirm the presence of GST. (Figure 4 and 3)

1000px

Figure 3. 0.85% agarose gel with GelRed. MW) NEB 1Kb Plus DNA Ladder, 13)Extraction GST BBa_K2719000, 14) Extraction GST BBa_K2719000 duplicate

User Reviews

UNIQf80ed41f19904041-partinfo-00000000-QINU UNIQf80ed41f19904041-partinfo-00000001-QINU

@@ Line 11: / Line 11: @@
 <p><i>Figure 1.</i> Transformed GST Colonies</p>
-To prove the presence of the plasmid inside the colonies, two agarose gels were elaborated, one for watch the entire plasmid and the second one for the plasmid with a previously restriction process using NotI, so the last one could confirm the presence of GST. (Figure 4 and 3)
+<p>To prove the presence of the plasmid inside the colonies, two agarose gels were elaborated, one for watch the entire plasmid and the second one for the plasmid with a previously restriction process using NotI, so the last one could confirm the presence of GST. (Figure 4 and 3)</p>
+[[file:T--TecCEM--GelK2719000|1000px]]
+<p><i>Figure 3.</i> 0.85% agarose gel with GelRed. MW) NEB 1Kb Plus DNA Ladder, 13)Extraction GST BBa_K2719000, 14) Extraction GST BBa_K2719000 duplicate</p>
 ===User Reviews===